Amino‐Terephthalonitrile and Amino‐Terephthalate‐Based Single Benzene Fluorophores – Compact Color Tunable Molecular Dyes for Bioimaging and Bioanalysis

Abstract

This review article discusses the emerging amino‐terephthalonitrile (Am‐TN) and amino terephthalate‐based single benzene fluorophores (SBFs) for their highly emissive nature and potential for numerous technical applications. Am‐TN‐SBFs are a new class of SBFs having amine as the electron donating (EDG) and dinitrile as the electron withdrawing group (EWG). The beauty of these Am‐TN‐SBFs lies in excellent intramolecular charge transfer between the EDG and EWG. The placement of two nitrile groups in para‐position on the benzene ring allows better charge transfer from the donating amines to the linear nitrile group leading to the strongly emissive nature. We also outline here the latest developments in the well‐known family of amino terephthalate SBFs reported in the last 2 to 3 years. Amino terephthalate SBFs have esters as the EWG and amine as the EDG. These have intramolecular H‐bonding between the EDG and EWG which is responsible for their emissive behavior.